Neurological disorders


Ontology type: npg:Subject  | skos:Concept     

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This table displays all metadata directly associated to this object as RDF triples.

820 TRIPLES      10 PREDICATES      54 URIs      11 LITERALS

Subject Predicate Object
1 sg:ontologies/subjects/neurological-disorders sgo:license sg:explorer/license/
2 sgo:sdDataset onto_subjects
3 rdf:type npg:Subject
4 skos:Concept
5 rdfs:label Neurological disorders
6 skos:altLabel Nervous System Disease
7 Nervous System Diseases
8 Nervous System Disorder
9 Nervous System Disorders
10 Neurologic Disorder
11 Neurologic Disorders
12 Neurological Disorder
13 skos:broader sg:ontologies/subjects/diseases
14 sg:ontologies/subjects/neurology
15 skos:definition Neurological disorders are disorders that affect the central nervous system or the peripheral nervous systems and can impair the brain, spinal cord, peripheral nerve or neuromuscular function.
16 skos:inScheme sg:ontologies/subjects/
17 skos:narrower sg:ontologies/subjects/brain-injuries
18 sg:ontologies/subjects/central-nervous-system-infections
19 sg:ontologies/subjects/cerebrovascular-disorders
20 sg:ontologies/subjects/cns-cancer
21 sg:ontologies/subjects/dementia
22 sg:ontologies/subjects/demyelinating-diseases
23 sg:ontologies/subjects/disorders-of-consciousness
24 sg:ontologies/subjects/dystonia
25 sg:ontologies/subjects/encephalopathy
26 sg:ontologies/subjects/epilepsy
27 sg:ontologies/subjects/headache
28 sg:ontologies/subjects/huntingtons-disease
29 sg:ontologies/subjects/hydrocephalus
30 sg:ontologies/subjects/hypoxic-ischaemic-encephalopathy
31 sg:ontologies/subjects/meningitis
32 sg:ontologies/subjects/migraine
33 sg:ontologies/subjects/motor-neuron-disease
34 sg:ontologies/subjects/movement-disorders
35 sg:ontologies/subjects/multiple-sclerosis
36 sg:ontologies/subjects/neural-tube-defects
37 sg:ontologies/subjects/neurodegeneration
38 sg:ontologies/subjects/neurodegenerative-diseases
39 sg:ontologies/subjects/neurodevelopmental-disorders
40 sg:ontologies/subjects/neuromuscular-disease
41 sg:ontologies/subjects/neuropathic-pain
42 sg:ontologies/subjects/neurotoxicity-syndromes
43 sg:ontologies/subjects/neurovascular-disorders
44 sg:ontologies/subjects/paediatric-neurological-disorders
45 sg:ontologies/subjects/parkinsons-disease
46 sg:ontologies/subjects/peripheral-neuropathies
47 sg:ontologies/subjects/prion-diseases
48 sg:ontologies/subjects/sleep-disorders
49 sg:ontologies/subjects/spinal-cord-diseases
50 sg:ontologies/subjects/spinocerebellar-ataxia
51 sg:ontologies/subjects/stroke
52 sg:ontologies/subjects/white-matter-disease
53 skos:prefLabel Neurological disorders
54 sg:ontologies/subjects/ dcterms:description The Nature Subjects Taxonomy is a polyhierarchical categorization of scholarly subject areas which are used for the indexing of content by Springer Nature.
55 dcterms:title Nature Subjects Taxonomy
56 sgo:sdDataset onto_subjects
57 rdf:type skos:ConceptScheme
58 skos:hasTopConcept sg:ontologies/subjects/DEPRECATED
59 sg:ontologies/subjects/biological-sciences
60 sg:ontologies/subjects/business-and-commerce
61 sg:ontologies/subjects/earth-and-environmental-sciences
62 sg:ontologies/subjects/health-sciences
63 sg:ontologies/subjects/humanities
64 sg:ontologies/subjects/physical-sciences
65 sg:ontologies/subjects/scientific-community-and-society
66 sg:ontologies/subjects/social-science
67 sg:ontologies/subjects/brain-injuries sgo:sdDataset onto_subjects
68 rdf:type npg:Subject
69 skos:Concept
70 rdfs:label Brain injuries
71 skos:altLabel Acute Brain Injuries
72 Acute Brain Injury
73 Brain Contusion
74 Brain Contusions
75 Brain Laceration
76 Brain Lacerations
77 Brain Trauma
78 Brain Traumas
79 Cortical Contusion
80 Cortical Contusions
81 Diffuse Brain Injuries
82 Diffuse Brain Injury
83 Focal Brain Injuries
84 Focal Brain Injury
85 Post Concussive Encephalopathy
86 Post Traumatic Encephalopathy
87 Post-Concussive Encephalopathies
88 Post-Concussive Encephalopathy
89 Post-Traumatic Encephalopathies
90 Post-Traumatic Encephalopathy
91 TBI (Traumatic Brain Injury)
92 TBIs (Traumatic Brain Injury)
93 Traumatic Brain Injuries
94 Traumatic Brain Injury
95 Traumatic Encephalopathies
96 Traumatic Encephalopathy
97 skos:broader sg:ontologies/subjects/neurological-disorders
98 skos:definition Brain injuries refer to a heterogeneous group of injuries that damage the brain. Common forms of brain injury include traumatic brain injury and stroke.
99 skos:inScheme sg:ontologies/subjects/
100 skos:narrower sg:ontologies/subjects/neonatal-brain-damage
101 sg:ontologies/subjects/white-matter-injury
102 skos:prefLabel Brain injuries
103 sg:ontologies/subjects/central-nervous-system-infections sgo:sdDataset onto_subjects
104 rdf:type npg:Subject
105 skos:Concept
106 rdfs:label Central nervous system infections
107 skos:altLabel Central Nervous System Infection
108 skos:broader sg:ontologies/subjects/neurological-disorders
109 skos:definition Central nervous system infections include bacterial and aseptic (typically viral) meningitis, viral and autoimmune encephalitis and myelitis, which targets the spinal cord.
110 skos:inScheme sg:ontologies/subjects/
111 skos:prefLabel Central nervous system infections
112 sg:ontologies/subjects/cerebrovascular-disorders sgo:sdDataset onto_subjects
113 rdf:type npg:Subject
114 skos:Concept
115 rdfs:label Cerebrovascular disorders
116 skos:altLabel Brain Vascular Disorder
117 Brain Vascular Disorders
118 Cerebrovascular Disease
119 Cerebrovascular Disorder
120 Cerebrovascular Insufficiencies
121 Cerebrovascular Insufficiency
122 Cerebrovascular Occlusion
123 Cerebrovascular Occlusions
124 Intracranial Vascular Disease
125 Intracranial Vascular Diseases
126 Intracranial Vascular Disorder
127 Intracranial Vascular Disorders
128 skos:broader sg:ontologies/subjects/neurological-disorders
129 sg:ontologies/subjects/vascular-diseases
130 skos:definition Cerebrovascular disorders are a group of pathological conditions in which impaired blood flow to the brain affects its function. Causes of cerebrovascular disorders include ischaemic and haemorrhagic stroke and malformations in the brain's arteries or veins.
131 skos:inScheme sg:ontologies/subjects/
132 skos:narrower sg:ontologies/subjects/stroke
133 skos:prefLabel Cerebrovascular disorders
134 sg:ontologies/subjects/cns-cancer sgo:sdDataset onto_subjects
135 rdf:type npg:Subject
136 skos:Concept
137 rdfs:label CNS cancer
138 skos:altLabel Central Nervous System Neoplasms
139 Central Nervous System Tumors
140 Primary Central Nervous System Neoplasms
141 skos:broader sg:ontologies/subjects/cancer
142 sg:ontologies/subjects/neurological-disorders
143 skos:definition CNS cancer is a type of cancer that forms in the central nervous system. It includes brain stem glioma, craniopharyngioma, medulloblastoma and meningioma.
144 skos:inScheme sg:ontologies/subjects/
145 skos:prefLabel CNS cancer
146 sg:ontologies/subjects/dementia sgo:sdDataset onto_subjects
147 rdf:type npg:Subject
148 skos:Concept
149 rdfs:label Dementia
150 skos:altLabel Amentia
151 Amentias
152 Dementias
153 Familial Dementia
154 Familial Dementias
155 Senile Paranoid Dementia
156 Senile Paranoid Dementias
157 skos:broader sg:ontologies/subjects/diseases-of-the-nervous-system
158 sg:ontologies/subjects/neurological-disorders
159 skos:definition Dementia is a syndrome that involves severe loss of cognitive abilities as a result of disease or injury. Dementia caused by traumatic brain injury is often static, whereas dementia caused by neurodegenerative disorders, such as Alzheimer's disease, is usually progressive and can eventually be fatal.
160 skos:inScheme sg:ontologies/subjects/
161 skos:narrower sg:ontologies/subjects/alzheimers-disease
162 skos:prefLabel Dementia
163 sg:ontologies/subjects/demyelinating-diseases sgo:sdDataset onto_subjects
164 rdf:type npg:Subject
165 skos:Concept
166 rdfs:label Demyelinating diseases
167 skos:altLabel Clinically Isolated CNS Demyelinating Syndrome
168 Demyelinating Disease
169 Demyelinating Disorder
170 Demyelinating Disorders
171 Demyelination
172 Demyelinations
173 skos:broader sg:ontologies/subjects/neurological-disorders
174 skos:definition Demyelinating diseases are a group of disorders of the nervous system that involve loss of the myelin sheath that normally surrounds the neurons. Demyelinating diseases can affect both the central nervous system and peripheral nervous system.
175 skos:inScheme sg:ontologies/subjects/
176 skos:narrower sg:ontologies/subjects/multiple-sclerosis
177 skos:prefLabel Demyelinating diseases
178 sg:ontologies/subjects/diseases sgo:sdDataset onto_subjects
179 rdf:type npg:Subject
180 skos:Concept
181 rdfs:label Diseases
182 skos:altLabel Disease
183 skos:broader sg:ontologies/subjects/health-sciences
184 skos:definition Diseases are abnormal conditions that have a specific set of signs and symptoms. Diseases can have an external cause, such as an infection, or an internal cause, such as autoimmune diseases.
185 skos:inScheme sg:ontologies/subjects/
186 skos:narrower sg:ontologies/subjects/cancer
187 sg:ontologies/subjects/cardiovascular-diseases
188 sg:ontologies/subjects/dental-diseases
189 sg:ontologies/subjects/endocrine-system-and-metabolic-diseases
190 sg:ontologies/subjects/eye-diseases
191 sg:ontologies/subjects/gastrointestinal-diseases
192 sg:ontologies/subjects/haematological-diseases
193 sg:ontologies/subjects/immunological-disorders
194 sg:ontologies/subjects/infectious-diseases
195 sg:ontologies/subjects/kidney-diseases
196 sg:ontologies/subjects/metabolic-disorders
197 sg:ontologies/subjects/neurological-disorders
198 sg:ontologies/subjects/nutrition-disorders
199 sg:ontologies/subjects/oral-diseases
200 sg:ontologies/subjects/psychiatric-disorders
201 sg:ontologies/subjects/reproductive-disorders
202 sg:ontologies/subjects/respiratory-tract-diseases
203 sg:ontologies/subjects/rheumatic-diseases
204 sg:ontologies/subjects/skin-diseases
205 sg:ontologies/subjects/trauma
206 sg:ontologies/subjects/urogenital-diseases
207 skos:prefLabel Diseases
208 sg:ontologies/subjects/disorders-of-consciousness sgo:sdDataset onto_subjects
209 rdf:type npg:Subject
210 skos:Concept
211 rdfs:label Disorders of consciousness
212 skos:altLabel Altered Level of Consciousness
213 Consciousness Disorder
214 Consciousness Disorders
215 Depressed Level of Consciousness
216 Semiconsciousness
217 skos:broader sg:ontologies/subjects/neurological-disorders
218 skos:definition Disorders of consciousness refer to medical conditions that impair the individual's ability for self-awareness and interaction with the environmental stimuli.
219 skos:inScheme sg:ontologies/subjects/
220 skos:prefLabel Disorders of consciousness
221 sg:ontologies/subjects/dystonia sgo:sdDataset onto_subjects
222 rdf:type npg:Subject
223 skos:Concept
224 rdfs:label Dystonia
225 skos:altLabel Diurnal Dystonia
226 Limb Dystonia
227 Muscle Dystonia
228 Paroxysmal Dystonia
229 skos:broader sg:ontologies/subjects/diseases-of-the-nervous-system
230 sg:ontologies/subjects/neurological-disorders
231 skos:definition Dystonia refers to a movement disorder characterized by abnormal posture or movements, caused by involuntary muscle contractions or cramps.
232 skos:inScheme sg:ontologies/subjects/
233 skos:prefLabel Dystonia
234 sg:ontologies/subjects/encephalopathy sgo:sdDataset onto_subjects
235 rdf:type npg:Subject
236 skos:Concept
237 rdfs:label Encephalopathy
238 skos:broader sg:ontologies/subjects/diseases-of-the-nervous-system
239 sg:ontologies/subjects/neurological-disorders
240 skos:definition Encephalopathy is a syndrome that involves global brain dysfunction. Encephalopathies have varying aetiologies: causes include for example ischaemic or traumatic brain injury, infectious agents, toxins, autoimmune attack or neurodegeneration.
241 skos:inScheme sg:ontologies/subjects/
242 skos:narrower sg:ontologies/subjects/hypoxic-ischaemic-encephalopathy
243 skos:prefLabel Encephalopathy
244 sg:ontologies/subjects/epilepsy sgo:sdDataset onto_subjects
245 rdf:type npg:Subject
246 skos:Concept
247 rdfs:label Epilepsy
248 skos:altLabel Aura
249 Auras
250 Awakening Epilepsy
251 Cryptogenic Epilepsies
252 Cryptogenic Epilepsy
253 Epilepsies
254 Epileptic Seizure
255 Epileptic Seizures
256 Seizure Disorder
257 Seizure Disorders
258 Single Seizure
259 Single Seizures
260 skos:broader sg:ontologies/subjects/diseases-of-the-nervous-system
261 sg:ontologies/subjects/neurological-disorders
262 skos:definition Epilepsy refers to a group of neurological disorders of varying aetiology, characterized by recurrent brain dysfunction that result from sudden excessive and disordered neuronal discharge. These episodes can manifest as epileptic seizures, but they can also occur with subtle or no behavioural signs.
263 skos:inScheme sg:ontologies/subjects/
264 skos:prefLabel Epilepsy
265 sg:ontologies/subjects/headache sgo:sdDataset onto_subjects
266 rdf:type npg:Subject
267 skos:Concept
268 rdfs:label Headache
269 skos:altLabel Bilateral Headache
270 Bilateral Headaches
271 Cephalalgia
272 Cephalalgias
273 Cephalgia
274 Cephalgias
275 Cephalodynia
276 Cephalodynias
277 Cranial Pain
278 Cranial Pains
279 Generalized Headache
280 Generalized Headaches
281 Head Pain
282 Head Pains
283 Headaches
284 Hemicrania
285 Ocular Headache
286 Ocular Headaches
287 Orthostatic Headache
288 Orthostatic Headaches
289 Periorbital Headache
290 Periorbital Headaches
291 Retro Ocular Headache
292 Retro-Ocular Headache
293 Retro-Ocular Headaches
294 Sharp Headache
295 Sharp Headaches
296 Throbbing Headache
297 Throbbing Headaches
298 Unilateral Headache
299 Unilateral Headaches
300 Vertex Headache
301 Vertex Headaches
302 skos:broader sg:ontologies/subjects/neurological-disorders
303 skos:definition Headache refers to pain of varying aetiology that is localized in the head and neck region. Most common reasons for primary headache are tension headache, migraine and neuropathic pain, such as trigeminal neuralgia. In secondary headache, the pain is a symptom of an underlying disorder.
304 skos:inScheme sg:ontologies/subjects/
305 skos:narrower sg:ontologies/subjects/migraine
306 skos:prefLabel Headache
307 sg:ontologies/subjects/huntingtons-disease sgo:sdDataset onto_subjects
308 rdf:type npg:Subject
309 skos:Concept
310 rdfs:label Huntington's disease
311 skos:altLabel Akinetic Rigid Variant of Huntington Disease
312 Akinetic-Rigid Variant of Huntington Disease
313 Chronic Progressive Hereditary Chorea (Huntington)
314 Huntington Chorea
315 Huntington Chronic Progressive Hereditary Chorea
316 Huntington disease
317 Huntington's Chorea
318 Juvenile Huntington Disease
319 Juvenile Onset Huntington Disease
320 Juvenile-Onset Huntington Disease
321 Late Onset Huntington Disease
322 Late-Onset Huntington Disease
323 skos:broader sg:ontologies/subjects/diseases-of-the-nervous-system
324 sg:ontologies/subjects/neurological-disorders
325 skos:definition Huntington's disease is a hereditary neurodegenerative disorder caused by an autosomal dominant mutation. The hallmark symptom of Huntington's disease is the presence of progressive chorea (abnormal involuntary movements), which is accompanied by psychiatric symptoms and cognitive decline.
326 skos:inScheme sg:ontologies/subjects/
327 skos:prefLabel Huntington's disease
328 sg:ontologies/subjects/hydrocephalus sgo:sdDataset onto_subjects
329 rdf:type npg:Subject
330 skos:Concept
331 rdfs:label Hydrocephalus
332 skos:altLabel Aqueductal Stenoses
333 Aqueductal Stenosis
334 Cerebral Ventriculomegalies
335 Cerebral Ventriculomegaly
336 Communicating Hydrocephalus
337 Congenital Hydrocephalus
338 Fetal Cerebral Ventriculomegalies
339 Fetal Cerebral Ventriculomegaly
340 Hydrocephalus Ex Vacuo
341 Hydrocephalus Ex-Vacuo
342 Hydrocephalus Ex-Vacuos
343 Hydrocephaly
344 Obstructive Hydrocephalus
345 Post Traumatic Hydrocephalus
346 Post-Traumatic Hydrocephalus
347 skos:broader sg:ontologies/subjects/neurological-disorders
348 skos:definition Hydrocephalus refers to the medical condition in which an excessive amount of cerebrospinal fluid accumulates within the cranium. It often results in enlarged cerebral ventricles and increased intracranial pressure, which can be fatal.
349 skos:inScheme sg:ontologies/subjects/
350 skos:prefLabel Hydrocephalus
351 sg:ontologies/subjects/hypoxic-ischaemic-encephalopathy sgo:sdDataset onto_subjects
352 rdf:type npg:Subject
353 skos:Concept
354 rdfs:label Hypoxic–ischaemic encephalopathy
355 skos:altLabel Hypoxic–ischemic encephalopathy
356 skos:broader sg:ontologies/subjects/encephalopathy
357 sg:ontologies/subjects/neurological-disorders
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359 skos:prefLabel Hypoxic–ischaemic encephalopathy
360 sg:ontologies/subjects/meningitis sgo:sdDataset onto_subjects
361 rdf:type npg:Subject
362 skos:Concept
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364 skos:altLabel Meningitides
365 Pachymeningitides
366 Pachymeningitis
367 skos:broader sg:ontologies/subjects/infectious-diseases
368 sg:ontologies/subjects/neurological-disorders
369 skos:definition Meningitis is an inflammatory disorder that is caused by infection of the meninges – the protective membranes that surround the central nervous system. Meningitis can be caused by bacterial or viral infections.
370 skos:inScheme sg:ontologies/subjects/
371 skos:prefLabel Meningitis
372 sg:ontologies/subjects/migraine sgo:sdDataset onto_subjects
373 rdf:type npg:Subject
374 skos:Concept
375 rdfs:label Migraine
376 skos:altLabel Abdominal Migraine
377 Abdominal Migraines
378 Acute Confusional Migraine
379 Acute Confusional Migraines
380 Cervical Migraine Syndrome
381 Cervical Migraine Syndromes
382 Hemicrania Migraine
383 Hemicrania Migraines
384 Migraine Disorder
385 Migraine Disorders
386 Migraine Headache
387 Migraine Headaches
388 Migraine Variant
389 Migraine Variants
390 Sick Headache
391 Sick Headaches
392 Status Migrainosus
393 skos:broader sg:ontologies/subjects/headache
394 sg:ontologies/subjects/neurological-disorders
395 skos:definition Migraine refers to a group of primary headache disorders marked by recurrent unilateral headache episodes. Migraine headache is often described as moderate to severe pulsating pain. Migraine can occur with or without preceding symptoms (referred to as aura) and is often accompanied by nausea and increased sensitivity to light.
396 skos:inScheme sg:ontologies/subjects/
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398 sg:ontologies/subjects/motor-neuron-disease sgo:sdDataset onto_subjects
399 rdf:type npg:Subject
400 skos:Concept
401 rdfs:label Motor neuron disease
402 skos:altLabel Amyotrophic Lateral Sclerosis
403 Anterior Horn Cell Disease
404 Familial Motor Neuron Disease
405 Lateral Scleroses
406 Lateral Sclerosis
407 Lower Motor Neuron Disease
408 Motor Neuron Diseases
409 Motor System Disease
410 Motor System Diseases
411 Primary Lateral Scleroses
412 Primary Lateral Sclerosis
413 Secondary Motor Neuron Disease
414 Upper Motor Neuron Disease
415 skos:broader sg:ontologies/subjects/neurodegenerative-diseases
416 sg:ontologies/subjects/neurological-disorders
417 skos:definition Motor neuron disease usually refers to amyotrophic lateral sclerosis, but it can also refer to other kind of neurodegenerative disease that affect the motor neurons, such as progressive primary lateral sclerosis, progressive muscular atrophy and progressive bulpar palsy.
418 skos:inScheme sg:ontologies/subjects/
419 skos:narrower sg:ontologies/subjects/amyotrophic-lateral-sclerosis
420 skos:prefLabel Motor neuron disease
421 sg:ontologies/subjects/movement-disorders sgo:sdDataset onto_subjects
422 rdf:type npg:Subject
423 skos:Concept
424 rdfs:label Movement disorders
425 skos:altLabel Etat Marbre
426 Lingual Facial Buccal Dyskinesia
427 Lingual-Facial-Buccal Dyskinesia
428 Lingual-Facial-Buccal Dyskinesias
429 Linguofacial Dyskinesia
430 Linguofacial Dyskinesias
431 Movement Disorder
432 Movement Disorder Syndrome
433 Movement Disorder Syndromes
434 Oral Dyskinesia
435 Oral Dyskinesias
436 Oral facial Dyskinesia
437 Oral-facial Dyskinesia
438 Oral-facial Dyskinesias
439 Orofacial Dyskinesia
440 Orofacial Dyskinesias
441 Status Marmoratus
442 Tardive Dyskinesia
443 Tardive Dyskinesias
444 Tardive Dystonia
445 Tardive Dystonias
446 Tardive Oral Dyskinesia
447 Tardive Oral Dyskinesias
448 skos:broader sg:ontologies/subjects/neurological-disorders
449 skos:definition Movement disorders are a group of neurological syndromes in which the hallmark symptom is paucity of movement, excessive and/or involuntary movement or tremor. Movement disorders can be neurodegenerative, such as Parkinson's disease and Huntington's disease, but they can also be induced by medication, infection, inflammation or trauma.
450 skos:inScheme sg:ontologies/subjects/
451 skos:narrower sg:ontologies/subjects/parkinsons-disease
452 skos:prefLabel Movement disorders
453 sg:ontologies/subjects/multiple-sclerosis sgo:sdDataset onto_subjects
454 rdf:type npg:Subject
455 skos:Concept
456 rdfs:label Multiple sclerosis
457 skos:altLabel Disseminated Sclerosis
458 MS (Multiple Sclerosis)
459 skos:broader sg:ontologies/subjects/autoimmune-diseases
460 sg:ontologies/subjects/demyelinating-diseases
461 sg:ontologies/subjects/diseases-of-the-nervous-system
462 sg:ontologies/subjects/myelin-biology-and-repair
463 sg:ontologies/subjects/neurological-disorders
464 sg:ontologies/subjects/white-matter-disease
465 skos:definition Multiple sclerosis is an autoimmune disease in which immune cells attack and destroy the protective myelin sheaths that surround nerve fibres, leading to neurological disturbances.
466 skos:inScheme sg:ontologies/subjects/
467 skos:prefLabel Multiple sclerosis
468 sg:ontologies/subjects/neural-tube-defects sgo:sdDataset onto_subjects
469 rdf:type npg:Subject
470 skos:Concept
471 rdfs:label Neural tube defects
472 skos:altLabel Acrania
473 Acranias
474 Craniorachischises
475 Craniorachischisis
476 Developmental Neural Tube Defects
477 Diastematomyelia
478 Diastematomyelias
479 Exencephalies
480 Exencephaly
481 Iniencephalies
482 Iniencephaly
483 Neural Tube Defect
484 Neural Tube Developmental Defects
485 Neurenteric Cyst
486 Neurenteric Cysts
487 Neuroenteric Cyst
488 Neuroenteric Cysts
489 Spinal Cord Myelodysplasia
490 Spinal Cord Myelodysplasias
491 Tethered Cord Syndrome
492 Tethered Cord Syndromes
493 skos:broader sg:ontologies/subjects/neurodevelopmental-disorders
494 sg:ontologies/subjects/neurological-disorders
495 skos:definition Neural tube defects result from a failure in closing of the neural tube during gastrulation, which causes congenital malformations of the spinal cord and brain. Open neural tube defects result in exposure of the brain and/or spinal cord at birth and include anencephaly, encephaloceles, hydranencephaly, iniencephaly, schizencephaly and spina bifida.
496 skos:inScheme sg:ontologies/subjects/
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502 skos:altLabel Nerve Degeneration
503 Nerve Degenerations
504 Neuron Degeneration
505 Neuron Degenerations
506 skos:broader sg:ontologies/subjects/diseases-of-the-nervous-system
507 sg:ontologies/subjects/neurological-disorders
508 skos:definition Neurodegeneration refers to the progressive atrophy and loss of function of neurons, which is present in neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease.
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510 skos:prefLabel Neurodegeneration
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512 rdf:type npg:Subject
513 skos:Concept
514 rdfs:label Neurodegenerative diseases
515 skos:altLabel Degenerative Neurologic Disease
516 Degenerative Neurologic Diseases
517 Degenerative Neurologic Disorder
518 Degenerative Neurologic Disorders
519 Nervous System Degenerative Diseases
520 Neurodegenerative Disease
521 Neurodegenerative Disorder
522 Neurodegenerative Disorders
523 Neurologic Degenerative Condition
524 Neurologic Degenerative Conditions
525 Neurologic Degenerative Disease
526 Neurologic Degenerative Diseases
527 skos:broader sg:ontologies/subjects/neurological-disorders
528 skos:definition Neurodegenerative diseases are a heterogeneous group of disorders that are characterized by the progressive degeneration of the structure and function of the central nervous system or peripheral nervous system. Common neurodegenerative diseases include Alzheimer's disease and Parkinson's disease.
529 skos:inScheme sg:ontologies/subjects/
530 skos:narrower sg:ontologies/subjects/alzheimers-disease
531 sg:ontologies/subjects/motor-neuron-disease
532 sg:ontologies/subjects/parkinsons-disease
533 sg:ontologies/subjects/prion-diseases
534 skos:prefLabel Neurodegenerative diseases
535 sg:ontologies/subjects/neurodevelopmental-disorders sgo:sdDataset onto_subjects
536 rdf:type npg:Subject
537 skos:Concept
538 rdfs:label Neurodevelopmental disorders
539 skos:broader sg:ontologies/subjects/genetics
540 sg:ontologies/subjects/neurological-disorders
541 skos:definition Neurodevelopmental disorders are a group of disorders in which the development of the central nervous system is disturbed. This can include developmental brain dysfunction, which can manifest as neuropsychiatric problems or impaired motor function, learning, language or non-verbal communication.
542 skos:inScheme sg:ontologies/subjects/
543 skos:narrower sg:ontologies/subjects/adhd
544 sg:ontologies/subjects/autism-spectrum-disorders
545 sg:ontologies/subjects/neural-tube-defects
546 skos:prefLabel Neurodevelopmental disorders
547 sg:ontologies/subjects/neurology sgo:sdDataset onto_subjects
548 rdf:type npg:Subject
549 skos:Concept
550 rdfs:label Neurology
551 skos:broader sg:ontologies/subjects/health-sciences
552 skos:definition Neurology is a medical specialty that is concerned with the study of structure, function and disorders of the nervous system.
553 skos:inScheme sg:ontologies/subjects/
554 skos:narrower sg:ontologies/subjects/neurological-disorders
555 skos:prefLabel Neurology
556 sg:ontologies/subjects/neuromuscular-disease sgo:sdDataset onto_subjects
557 rdf:type npg:Subject
558 skos:Concept
559 rdfs:label Neuromuscular disease
560 skos:altLabel Amyotonia Congenita
561 Benign Fasciculation-Cramp Syndrome
562 Benign Fasciculation-Cramp Syndromes
563 Cramp Fasciculation Syndrome
564 Cramp-Fasciculation Syndrome
565 Cramp-Fasciculation Syndromes
566 Foley Denny Brown Syndrome
567 Foley-Denny-Brown Syndrome
568 Neuromuscular Disorder
569 Oppenheim Disease
570 Oppenheim's Disease
571 Oppenheims Disease
572 skos:broader sg:ontologies/subjects/neurological-disorders
573 skos:definition Neuromuscular disease refers to a group of heterogeneous disorders that impair the function of motor nerves, muscles or neuromuscular junctions. Symptoms can include muscle pain, weakness or atrophy, fasciculations or spasms, hypertonia and hypotonia.
574 skos:inScheme sg:ontologies/subjects/
575 skos:prefLabel Neuromuscular disease
576 sg:ontologies/subjects/neuropathic-pain sgo:sdDataset onto_subjects
577 rdf:type npg:Subject
578 skos:Concept
579 rdfs:label Neuropathic pain
580 skos:altLabel Atypical Neuralgia
581 Atypical Neuralgias
582 Iliohypogastric Nerve Neuralgia
583 Iliohypogastric Nerve Neuralgias
584 Ilioinguinal Neuralgia
585 Ilioinguinal Neuralgias
586 Nerve Pain
587 Nerve Pains
588 Neuralgia
589 Neuralgias
590 Neurodynia
591 Neurodynias
592 Neuropathic Pains
593 Paroxysmal Nerve Pain
594 Paroxysmal Nerve Pains
595 Perineal Neuralgia
596 Perineal Neuralgias
597 Stump Neuralgia
598 Stump Neuralgias
599 Supraorbital Neuralgia
600 Supraorbital Neuralgias
601 Vidian Neuralgia
602 Vidian Neuralgias
603 skos:broader sg:ontologies/subjects/neurological-disorders
604 skos:definition Neuropathic pain is caused by disorders of, or damage to, the nervous system. The affected nerves can induce the sensation of pain in the brain. Neuropathic pain is often associated with the sensation of burning, coldness, "pins and needles", numbness or itching.
605 skos:inScheme sg:ontologies/subjects/
606 skos:prefLabel Neuropathic pain
607 sg:ontologies/subjects/neurotoxicity-syndromes sgo:sdDataset onto_subjects
608 rdf:type npg:Subject
609 skos:Concept
610 rdfs:label Neurotoxicity syndromes
611 skos:altLabel Nervous System Poisoning
612 Nervous System Poisonings
613 Neurotoxic Disorder
614 Neurotoxic Disorders
615 Neurotoxicity Syndrome
616 Neurotoxin Disease
617 Neurotoxin Diseases
618 Neurotoxin Disorder
619 Neurotoxin Disorders
620 Toxic Encephalitides
621 Toxic Encephalitis
622 Toxic Encephalopathies
623 Toxic Encephalopathy
624 skos:broader sg:ontologies/subjects/neurological-disorders
625 skos:definition Neurotoxicity syndromes are neurological disorders that result from exposure to neurotoxic substances, such as pharmaceutical agents, pesticides, solvents, heavy metals, radiation or naturally occurring neurotoxic substances such as bacterial toxins.
626 skos:inScheme sg:ontologies/subjects/
627 skos:prefLabel Neurotoxicity syndromes
628 sg:ontologies/subjects/neurovascular-disorders sgo:sdDataset onto_subjects
629 rdf:type npg:Subject
630 skos:Concept
631 rdfs:label Neurovascular disorders
632 skos:broader sg:ontologies/subjects/neurological-disorders
633 skos:definition Neurovascular disorders are a group of pathological conditions that result from infarction, ischaemic or haemorrhagic stroke of the brain or the spinal cord.
634 skos:inScheme sg:ontologies/subjects/
635 skos:narrower sg:ontologies/subjects/stroke
636 skos:prefLabel Neurovascular disorders
637 sg:ontologies/subjects/paediatric-neurological-disorders sgo:sdDataset onto_subjects
638 rdf:type npg:Subject
639 skos:Concept
640 rdfs:label Paediatric neurological disorders
641 skos:broader sg:ontologies/subjects/neurological-disorders
642 skos:definition Paediatric neurological disorders refer to those disorders of the nervous system that affect children.
643 skos:inScheme sg:ontologies/subjects/
644 skos:narrower sg:ontologies/subjects/neonatal-brain-damage
645 sg:ontologies/subjects/retinopathy-of-prematurity
646 skos:prefLabel Paediatric neurological disorders
647 sg:ontologies/subjects/parkinsons-disease sgo:sdDataset onto_subjects
648 rdf:type npg:Subject
649 skos:Concept
650 rdfs:label Parkinson's disease
651 skos:altLabel Idiopathic Parkinson Disease
652 Idiopathic Parkinson's Disease
653 Idiopathic Parkinsonism
654 Lewy Body Parkinson Disease
655 Lewy Body Parkinson's Disease
656 Paralysis Agitans
657 Parkinson Disease
658 Primary Parkinsonism
659 skos:broader sg:ontologies/subjects/diseases-of-the-nervous-system
660 sg:ontologies/subjects/movement-disorders
661 sg:ontologies/subjects/neurodegenerative-diseases
662 sg:ontologies/subjects/neurological-disorders
663 skos:definition Parkinson's disease is a progressive neurodegenerative disorder, which is characterized by motor symptoms such as tremor, rigidity, slowness of movement and problems with gait. Motor symptoms are often accompanied with fatigue, depression, pain and cognitive problems.
664 skos:inScheme sg:ontologies/subjects/
665 skos:prefLabel Parkinson's disease
666 sg:ontologies/subjects/peripheral-neuropathies sgo:sdDataset onto_subjects
667 rdf:type npg:Subject
668 skos:Concept
669 rdfs:label Peripheral neuropathies
670 skos:altLabel PNS (Peripheral Nervous System) Diseases
671 PNS Disease
672 PNS Diseases
673 Peripheral Nerve Disease
674 Peripheral Nerve Diseases
675 Peripheral Nervous System Disease
676 Peripheral Nervous System Diseases
677 Peripheral Nervous System Disorders
678 Peripheral Neuropathy
679 skos:broader sg:ontologies/subjects/neurological-disorders
680 skos:definition Peripheral neuropathies are a group of diseases that cause acute and/or chronic impairment or damage to the nerves belonging to the peripheral nervous system, such as motor nerves or sensory nerves.
681 skos:inScheme sg:ontologies/subjects/
682 skos:prefLabel Peripheral neuropathies
683 sg:ontologies/subjects/prion-diseases sgo:sdDataset onto_subjects
684 rdf:type npg:Subject
685 skos:Concept
686 rdfs:label Prion diseases
687 skos:altLabel Inherited Human Transmissible Spongiform Encephalopathies
688 Prion Disease
689 Prion Induced Disorder
690 Prion Protein Disease
691 Prion Protein Diseases
692 Prion-Induced Disorder
693 Prion-Induced Disorders
694 Transmissible Dementia
695 Transmissible Dementias
696 Transmissible Spongiform Encephalopathies
697 Transmissible Spongiform Encephalopathy
698 skos:broader sg:ontologies/subjects/neurodegenerative-diseases
699 sg:ontologies/subjects/neurological-disorders
700 skos:definition Prion diseases are a group of progressive neurodegenerative diseases that are caused by misfolded proteins, referred to as prions. During post-translational modification of proteins, prions act as a folding template, converting proteins into infectious prion form. The best-known human prion disease is Creutzfeld–Jakob disease.
701 skos:inScheme sg:ontologies/subjects/
702 skos:prefLabel Prion diseases
703 sg:ontologies/subjects/sleep-disorders sgo:sdDataset onto_subjects
704 rdf:type npg:Subject
705 skos:Concept
706 rdfs:label Sleep disorders
707 skos:altLabel Dyssomnia
708 Long Sleeper Syndrome
709 Long Sleeper Syndromes
710 Short Sleeper Syndrome
711 Short Sleeper Syndromes
712 Sleep Related Neurogenic Tachypnea
713 Sleep-Related Neurogenic Tachypnea
714 Sleep-Related Neurogenic Tachypneas
715 Somnipathies
716 Subwakefullness Syndrome
717 Subwakefullness Syndromes
718 skos:broader sg:ontologies/subjects/neurological-disorders
719 skos:definition Sleep disorders are a group of conditions in which the normal sleep pattern or sleep behaviours are disturbed. Primary sleep disorders include insomnia, hypersomnia, obstructive sleep apnoea and parasomnias (abnormal sleep behaviours, such as sleepwalking and rapid eye movement sleep behaviour disorder).
720 skos:inScheme sg:ontologies/subjects/
721 skos:prefLabel Sleep disorders
722 sg:ontologies/subjects/spinal-cord-diseases sgo:sdDataset onto_subjects
723 rdf:type npg:Subject
724 skos:Concept
725 rdfs:label Spinal cord diseases
726 skos:altLabel Myelopathies
727 Myelopathy
728 Spinal Cord Disease
729 Spinal Cord Disorder
730 Spinal Cord Disorders
731 skos:broader sg:ontologies/subjects/neurological-disorders
732 skos:definition Spinal cord diseases are a heterogeneous group of conditions that cause damage or dysfunction of the spinal cord. They include infections, inflammatory disorders, vascular diseases and disorders that affect the meninges or perimeningeal spaces that surround the spinal cord.
733 skos:inScheme sg:ontologies/subjects/
734 skos:prefLabel Spinal cord diseases
735 sg:ontologies/subjects/spinocerebellar-ataxia sgo:sdDataset onto_subjects
736 rdf:type npg:Subject
737 skos:Concept
738 rdfs:label Spinocerebellar ataxia
739 skos:altLabel Dominantly Inherited Spinocerebellar Ataxias
740 Dominantly-Inherited Spinocerebellar Ataxia
741 Dominantly-Inherited Spinocerebellar Ataxias
742 Spinocerebellar Ataxia 1
743 Spinocerebellar Ataxia 2
744 Spinocerebellar Ataxia 4
745 Spinocerebellar Ataxia 5
746 Spinocerebellar Ataxia 6
747 Spinocerebellar Ataxia 7
748 Spinocerebellar Ataxia Type 1
749 Spinocerebellar Ataxia Type 2
750 Spinocerebellar Ataxia Type 4
751 Spinocerebellar Ataxia Type 5
752 Spinocerebellar Ataxia Type 6
753 Spinocerebellar Ataxia Type 7
754 Spinocerebellar Ataxia-1
755 Spinocerebellar Ataxia-2
756 Spinocerebellar Ataxia-4
757 Spinocerebellar Ataxia-5
758 Spinocerebellar Ataxia-6
759 Spinocerebellar Ataxia-7
760 Spinocerebellar Ataxias
761 Spinocerebellar Atrophies
762 Spinocerebellar Atrophy
763 Type 1 Spinocerebellar Ataxia
764 Type 2 Spinocerebellar Ataxia
765 Type 4 Spinocerebellar Ataxia
766 Type 5 Spinocerebellar Ataxia
767 Type 6 Spinocerebellar Ataxia
768 Type 7 Spinocerebellar Ataxia
769 skos:broader sg:ontologies/subjects/diseases-of-the-nervous-system
770 sg:ontologies/subjects/neurological-disorders
771 skos:definition Spinocerebellar ataxia refers to a group of genetic, progressive neurodegenerative disorders of the spine and the cerebellum that can affect balance, coordination and speech.
772 skos:inScheme sg:ontologies/subjects/
773 skos:prefLabel Spinocerebellar ataxia
774 sg:ontologies/subjects/stroke sgo:sdDataset onto_subjects
775 rdf:type npg:Subject
776 skos:Concept
777 rdfs:label Stroke
778 skos:altLabel Acute Cerebrovascular Accident
779 Acute Cerebrovascular Accidents
780 Acute Stroke
781 Acute Strokes
782 Apoplexy
783 Brain Vascular Accident
784 Brain Vascular Accidents
785 CVA (Cerebrovascular Accident)
786 CVAs (Cerebrovascular Accident)
787 Cerebral Stroke
788 Cerebral Strokes
789 Cerebrovascular Accident
790 Cerebrovascular Accidents
791 Cerebrovascular Apoplexy
792 Cerebrovascular Stroke
793 Cerebrovascular Strokes
794 Strokes
795 skos:broader sg:ontologies/subjects/cerebrovascular-disorders
796 sg:ontologies/subjects/diseases-of-the-nervous-system
797 sg:ontologies/subjects/neurological-disorders
798 sg:ontologies/subjects/neurovascular-disorders
799 skos:definition Stroke refers to an acute cerebrovascular disorder that is manifested by sudden loss or deterioration of brain function, resulting either from ischaemic stroke or intracranial haemorrhage.
800 skos:inScheme sg:ontologies/subjects/
801 skos:prefLabel Stroke
802 sg:ontologies/subjects/white-matter-disease sgo:sdDataset onto_subjects
803 rdf:type npg:Subject
804 skos:Concept
805 rdfs:label White matter disease
806 skos:altLabel Childhood Ataxia with Diffuse Central Nervous System Hypomyelination
807 Leukoencephalopathies
808 Leukoencephalopathy
809 Leukoencephalopathy with Vanishing White Matter
810 White Matter Diseases
811 skos:broader sg:ontologies/subjects/neurological-disorders
812 skos:definition White matter disease refers to a group of heterogeneous disorders that involve degeneration of the white matter of the brain.
813 skos:inScheme sg:ontologies/subjects/
814 skos:narrower sg:ontologies/subjects/multiple-sclerosis
815 skos:prefLabel White matter disease
816 skos:Concept sgo:sdDataset for_codes
817 rdf:type rdfs:Class
818 rdfs:Resource
819 rdfs:subClassOf rdfs:Resource
820 skos:Concept
 




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